These and some of our further results demonstrate that the 4,5-dibydropyridazine tautomer (e.g. 1%') is the less stable isomer in the series of cycloaddition products from vinylindoles with 3 (see also [Sc]). ') 4, This value correlates with the first vertical ionization potential obtained from He(1
β¦ LIBER β¦
First cycloaddition of 2-vinylindoles with dimethyl, 1,2,4,5-tetrazine-3,6-dicarboxylate: Diels-Alder reactions with inverse electron demand to new substituted and annelated pyridazines
β Scribed by Ulf Pindur; Myung-Hwa Kim
- Book ID
- 108381657
- Publisher
- Elsevier Science
- Year
- 1988
- Tongue
- French
- Weight
- 155 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0040-4039
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